Validation Engineer

United Consulting Hub; Illinois; On-site; USD 65,000 - 85,000; Full time

Job summary

United Consulting Hub is seeking a Validation Engineer in Illinois to support validation activities within a regulated medical device manufacturing environment. This position is perfect for recent graduates or early-career professionals who are interested in process validation and quality compliance.

The role involves assisting with process validation activities, supporting validation protocols, and collaborating with various teams to maintain compliance with FDA and ISO standards.

Qualifications

• BS in Engineering, Life Sciences, or a related field.
• Basic understanding of validation concepts (IQ/OQ/PQ).
• Strong documentation and communication skills.

Responsibilities

• Assist with Process Validation activities (IQ/OQ/PQ).
• Support execution of validation protocols and reports.
• Participate in equipment qualification and testing activities.
• Collaborate with Quality, Manufacturing, and Engineering teams.

Skills

Process Validation

Documentation Skills

Analytical Skills

Communication Skills

Education

BS in Engineering, Life Sciences, or related field

Job description

We are seeking a Validation Engineer to support validation activities within a regulated medical device manufacturing environment. This role is ideal for recent graduates or early-career professionals interested in process validation, equipment qualification, and quality compliance.

Key Responsibilities:

• Assist with Process Validation activities (IQ/OQ/PQ)
• Support execution of validation protocols and reports
• Participate in equipment qualification and testing activities
• Collaborate with Quality, Manufacturing, and Engineering teams
• Maintain validation documentation in compliance with FDA and ISO requirements
• Support investigations, CAPAs, and continuous improvement initiatives

Qualifications:

• BS in Engineering, Life Sciences, or a related field
• Basic understanding of validation concepts (IQ/OQ/PQ)
• Knowledge of FDA regulations and ISO 13485 preferred
• Strong documentation, analytical, and communication skills
• Internship or project experience in medical devices or regulated industries is a plus